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Recruiting
NCT05599776
The Effect of Smart Ring Assisted Physiotherapeutic Intervention After TKR
Conditions: Osteo Arthritis Knee
Sex: All
Ages: 18 Years – 70 Years
Phase: NA
Enrollment: 338
Sponsor: Coxa, Hospital for Joint Replacement
Location: Finland
Summary
The goal of this randomized controlled trial is to learn about the effect of a wearable activity tracker assisted physiotherapeutic intervention on the risk of poor patient reported outcome after a primary total knee replacement.The main question it aims to answer is whether a wearable activity tracker assisted physiotherapeutic intervention and remote monitoring may help to decrease the number of the poor patient reported post-operative outcome 12 months after a primary total knee replacement.Participants will receive standard postoperative care which includes physiotherapy appointments 4 weeks and 3 months after the surgery and they will use smart rings (Oura ring) 3 months postoperatively.
Patients will be remotely monitored to follow their recovery from total knee replacement surgery: the study group physiotherapists will follow the patients' activity and sleep and if necessary, make a contact with patient if there seems to low activity indicating difficulties with recovering from the surgery.Researchers will compare the intervention group to a group of participants who will receive only standard postoperative care with physiotherapy appointments 4 weeks and 3 months, to see if the use of the Oura ring may decrease the number of participants with poor patient reported post-operative outcome after total knee replacement.
Eligibility Criteria
Inclusion Criteria:Patients undergoing primary TKA for primary osteoarthritis.Patients able to consent and willing to comply with the study protocol.Patients aged 18 to 70 yearsPatients is able to use a smartphone and a smart ring.Exclusion Criteria:Patients unwilling to provide informed consent>15 degrees varus or valgus, or > 15 degrees fixed flexion deformityPhysical, emotional, or neurological conditions that would compromise the patient, e.g., poor compliance with postoperative rehabilitation and follow-up (e.g., drug or alcohol abuse, serious mental illness, general neurological conditions, such as Parkinson, MS, etc.)Patients unable to attend the study physiotherapy appointments at the outpatient clinic.Patients unable to wear Oura ring (example in case of OA or rheumatoid arthritis in the finger joints).Patients with cardiac arrhythmia.
Source: ClinicalTrials.gov (NCT05599776). StuddyBuddy aggregates publicly available trial information.